Your browser doesn't support javascript.
loading
Visual and absorbance analyses of admixtures containing vancomycin and piperacillin-tazobactam at commonly used concentrations.
O'Donnell, J Nicholas; Venkatesan, Natarajan; Manek, Malav; Rhodes, Nathaniel J; Scheetz, Marc H.
Afiliação
  • O'Donnell JN; Department of Pharmacy Practice, Chicago College of Pharmacy, Midwestern University, Downers Grove, IL, and Department of Pharmacy, Northwestern Memorial Hospital, Chicago, IL.
  • Venkatesan N; Department of Pharmaceutical Science, Chicago College of Pharmacy, Midwestern University, Downers Grove, IL.
  • Manek M; Chicago College of Pharmacy, Midwestern University, Downers Grove, IL.
  • Rhodes NJ; Department of Pharmacy Practice, Chicago College of Pharmacy, Midwestern University, Downers Grove, IL, and Department of Pharmacy, Northwestern Memorial Hospital, Chicago, IL.
  • Scheetz MH; Department of Pharmacy Practice, Chicago College of Pharmacy, Midwestern University, Downers Grove, IL, and Department of Pharmacy, Northwestern Memorial Hospital, Chicago, IL. mscheetz@nm.org.
Am J Health Syst Pharm ; 73(4): 241-6, 2016 Feb 15.
Article em En | MEDLINE | ID: mdl-26843502
ABSTRACT

PURPOSE:

The compatibility of vancomycin and piperacillin-tazobactam in concentrations typically used in extended-infusion dosing schemes was evaluated.

METHODS:

Piperacillin-tazobactam was reconstituted and diluted to concentrations of 33.75, 45, 50, 60, 67.5, 80, and 90 mg/mL. Vancomycin was diluted to concentrations of 4-8, 10, and 12 mg/mL. The resultant admixtures were visually observed after preparation against black and white backgrounds each hour between hours 1 through 4 and after 24 hours. Frozen products of each medication and brand-name Zosyn powder for reconstitution also were studied. Each combination of products and concentrations was tested for precipitation using simulated Y-site administration. Absorbance and microscopic analyses were performed to discern less perceptible incompatibilities in combinations that did not result in visual precipitation. Changes in absorbance were evaluated using two-way repeated-measures analysis of variance with post hoc Bonferroni corrections.

RESULTS:

No tested concentrations of piperacillin-tazobactam showed precipitations with vancomycin up to concentrations of 7 mg/mL. Piperacillin-tazobactam 80-90 mg/mL formed reversible precipitation with vancomycin 8 mg/mL. All tested concentrations of piperacillin-tazobactam formed a reversible precipitate with vancomycin 10 mg/mL. Irreversible precipitation was noted with all combinations of piperacillin-tazobactam and vancomycin 12 mg/mL. No significant changes in absorbance analyses were identified for all tested piperacillin-tazobactam concentrations and vancomycin 4-10 mg/mL compared with 0.9% sodium chloride injection (p > 0.05). Similar results were observed using frozen preparations and brand-name Zosyn.

CONCLUSION:

Visual, microscopic, and absorbance analyses showed no evidence of incompatibility when piperacillin-tazobactam 33.75-90 mg/mL was combined with vancomycin ≤7 mg/mL. Reversible and irreversible precipitates formed when piperacillin-tazobactam was combined with vancomycin ≥8 mg/mL.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vancomicina / Ácido Penicilânico / Antibacterianos Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vancomicina / Ácido Penicilânico / Antibacterianos Idioma: En Ano de publicação: 2016 Tipo de documento: Article